Inductively coupled plasma mass spectrometry to identify protein drug targets from whole cell systems

Claire S. Allardyce; Paul J. Dyson; Fadi R. Abou-Shakra; Heather Birtwistle; Jonathan Coffey

doi:10.1039/B108418F

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Chemical Communications

Issue 24, 2001

Urgent high quality communications from across the chemical sciences.

Impact Factor 6.169 100 Issues per Year Indexed in MEDLINE

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Inductively coupled plasma mass spectrometry to identify protein drug targets from whole cell systems

Claire S. Allardyce,^a Paul J. Dyson,*^a Fadi R. Abou-Shakra,^b Heather Birtwistle^b and Jonathan Coffey^b

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Department of Chemistry, The University of York, Heslington, York, UK
E-mail: pjd14@york.ac.uk

Micromass UK Ltd, Atlas Park, Simonsway, Manchester, UK

Chem. Commun., 2001, 2708-2709

DOI: 10.1039/B108418F
Received 19 Sep 2001, Accepted 14 Nov 2001
First published online 07 Dec 2001

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Abstract
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Proteins from cisplatin treated bacterial cells were partially separated by 1D polyacrylamide gel electrophoresis and analysed by laser ablation inductively coupled plasma mass spectrometry; using peptide fingerprinting methods central to proteomics, the band containing the highest levels of platinum was found to contain outer membrane protein A, which may be involved in cisplatin uptake.

Abstract from Mass Spectrometry Bulletin 2002

Biochemical, Inductively coupled plasma/MS, Laser - other uses, Structure confirmation, Laser ablation, Escherichia coli.

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Supplementary Info

Full details of laser ablation ICP-MS and QTOF operating conditions, further experimental details for peptide separation and peptide sequencing maps for OmpA
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Claire S. Allardyce
Paul J. Dyson
Fadi R. Abou-Shakra
Heather Birtwistle
Jonathan Coffey

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Inductively coupled plasma mass spectrometry to identify protein drug targets from whole cell systems

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